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Agnosic alexia
Alexia
Alexia with agraphia
Alexia with agraphia of the inferior parietal lobule
Alexia without agraphia
Alexia without aphasia
Alexic agnosia
Aphasic alexia
Associated alexia
Cortical alexia
Isolated alexia
Isolated autosomal dominant hypomagnesemia
Literal alexia
Occipital alexia
Optic aphasia
Optical alexia
Parietal alexia
Primary alexia
Pure alexia
Sensory alexia
Symbolic alexia
Verbal alexia
Visual agnosic alexia
Visual alexia
Visual cortical alexia
Word blindness

Vertaling van "Isolated alexia " (Engels → Frans) :

optic aphasia | agnosic alexia | alexic agnosia | alexia without agraphia | alexia without aphasia | literal alexia | occipital alexia | optical alexia | primary alexia | pure alexia | sensory alexia | symbolic alexia | verbal alexia | visual alexia | visual agnosic alexia | word blindness | isolated alexia

aphasie optique | alexie agnosique | agnosie alexique | alexie sans agraphie | alexie sans aphasie | alexie littérale | alexie occipitale | alexie optique | alexie primaire | alexie pure | alexie sensorielle | alexie symbolique | alexie verbale | alexie visuelle | alexie agnosique visuelle | cécité verbale | alexie isolée


alexia with agraphia of the inferior parietal lobule | aphasic alexia | parietal alexia | visual cortical alexia

alexie avec agraphie dite du pli courbe | alexie aphasique | alexie corticale visuelle | alexie pariétale


alexia with agraphia | associated alexia | cortical alexia

alexie avec agraphie | alexie associée | alexie corticale


A very rare genetic vascular disease of autosomal recessive inheritance, described in less than 20 patients to date. The disease has manifestations of adult-onset (as early as the second decade of life) isolated calcification of the arteries of the l

syndrome héréditaire de calcification artérielle et articulaire




Isolated autosomal dominant hypomagnesemia

hypomagnésémie primaire autosomique dominante avec hypocalciurie


A cerebral malformation with epilepsy with predominant characteristics of posterior isolated lissencephaly with developmental delay, intellectual disability and epilepsy that usually evolves from West syndrome to Lennox-Gastaut syndrome. Additional f

lissencéphalie par mutation de LIS1




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'Isolated alexia' ->

Date index: 2024-05-18
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